Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 36 of 90 entries
Sorted by: Best Match Show Resources per page
HMGA1a Induces Alternative Splicing of the .

Frontiers in molecular biosciences

Ohe K, Miyajima S, Tanaka T, Hamaguchi Y, Harada Y, Horita Y, Beppu Y, Ito F, Yamasaki T, Terai H, Mori M, Murata Y, Tanabe M, Abe I, Ashida K, Kobayashi K, Enjoji M, Nomiyama T, Yanase T, Harada N, Utsumi T, Mayeda A.
PMID: 29938207
Front Mol Biosci. 2018 Jun 08;5:52. doi: 10.3389/fmolb.2018.00052. eCollection 2018.

No abstract available.

Cite
Ohe K, Miyajima S, Tanaka T, et al. HMGA1a Induces Alternative Splicing of the . Front Mol Biosci. 2018;5:52doi: 10.3389/fmolb.2018.00052.
Ohe, K., Miyajima, S., Tanaka, T., Hamaguchi, Y., Harada, Y., Horita, Y., Beppu, Y., Ito, F., Yamasaki, T., Terai, H., Mori, M., Murata, Y., Tanabe, M., Abe, I., Ashida, K., Kobayashi, K., Enjoji, M., Nomiyama, T., Yanase, T., Harada, N., Utsumi, T., & Mayeda, A. (2018). HMGA1a Induces Alternative Splicing of the . Frontiers in molecular biosciences, 552. https://doi.org/10.3389/fmolb.2018.00052
Ohe, Kenji, et al. "HMGA1a Induces Alternative Splicing of the ." Frontiers in molecular biosciences vol. 5 (2018): 52. doi: https://doi.org/10.3389/fmolb.2018.00052
Ohe K, Miyajima S, Tanaka T, Hamaguchi Y, Harada Y, Horita Y, Beppu Y, Ito F, Yamasaki T, Terai H, Mori M, Murata Y, Tanabe M, Abe I, Ashida K, Kobayashi K, Enjoji M, Nomiyama T, Yanase T, Harada N, Utsumi T, Mayeda A. HMGA1a Induces Alternative Splicing of the . Front Mol Biosci. 2018 Jun 08;5:52. doi: 10.3389/fmolb.2018.00052. eCollection 2018. PMID: 29938207; PMCID: PMC6002489.
Copy Download .nbib Format: NLM
Establishment of a Novel Model for Anticancer Drug Resistance in Three-Dimensional Primary Culture of Tumor Microenvironment.

Stem cells international

Usui T, Sakurai M, Enjoji S, Kawasaki H, Umata K, Ohama T, Fujiwara N, Yabe R, Tsuji S, Yamawaki H, Hazama S, Takenouchi H, Nakajima M, Tsunedomi R, Suzuki N, Nagano H, Sato K.
PMID: 28119740
Stem Cells Int. 2016;2016:7053872. doi: 10.1155/2016/7053872. Epub 2016 Dec 29.

Tumor microenvironment has been implicated in tumor development and progression. As a three-dimensional tumor microenvironment model, air liquid interface (ALI) organoid culture from oncogene transgenic mouse gastrointestinal tissues was recently produced. However, ALI organoid culture system from tissues of...

Cite
Usui T, Sakurai M, Enjoji S, et al. Establishment of a Novel Model for Anticancer Drug Resistance in Three-Dimensional Primary Culture of Tumor Microenvironment. Stem Cells Int. 2016;2016:7053872doi: 10.1155/2016/7053872.
Usui, T., Sakurai, M., Enjoji, S., Kawasaki, H., Umata, K., Ohama, T., Fujiwara, N., Yabe, R., Tsuji, S., Yamawaki, H., Hazama, S., Takenouchi, H., Nakajima, M., Tsunedomi, R., Suzuki, N., Nagano, H., & Sato, K. (2016). Establishment of a Novel Model for Anticancer Drug Resistance in Three-Dimensional Primary Culture of Tumor Microenvironment. Stem cells international, 20167053872. https://doi.org/10.1155/2016/7053872
Usui, Tatsuya, et al. "Establishment of a Novel Model for Anticancer Drug Resistance in Three-Dimensional Primary Culture of Tumor Microenvironment." Stem cells international vol. 2016 (2016): 7053872. doi: https://doi.org/10.1155/2016/7053872
Usui T, Sakurai M, Enjoji S, Kawasaki H, Umata K, Ohama T, Fujiwara N, Yabe R, Tsuji S, Yamawaki H, Hazama S, Takenouchi H, Nakajima M, Tsunedomi R, Suzuki N, Nagano H, Sato K. Establishment of a Novel Model for Anticancer Drug Resistance in Three-Dimensional Primary Culture of Tumor Microenvironment. Stem Cells Int. 2016;2016:7053872. doi: 10.1155/2016/7053872. Epub 2016 Dec 29. PMID: 28119740; PMCID: PMC5227181.
Copy Download .nbib Format: NLM
Spin-stripe density varies linearly with the hole content in single-layer Bi2+xSr2-xCuO6+y cuprate superconductors.

Physical review letters

Enoki M, Fujita M, Nishizaki T, Iikubo S, Singh DK, Chang S, Tranquada JM, Yamada K.
PMID: 23383829
Phys Rev Lett. 2013 Jan 04;110(1):017004. doi: 10.1103/PhysRevLett.110.017004. Epub 2013 Jan 02.

We have performed inelastic neutron scattering measurements on the single-layer cuprate Bi(2+x) Sr(2-x) CuO(6+y) (Bi2201) with x = 0.2, 0.3, 0.4, and 0.5, a doping range that spans the spin-glass to superconducting phase boundary. The doping evolution of low...

Cite
Enoki M, Fujita M, Nishizaki T, et al. Spin-stripe density varies linearly with the hole content in single-layer Bi2+xSr2-xCuO6+y cuprate superconductors. Phys Rev Lett. 2013;110(1):017004doi: 10.1103/PhysRevLett.110.017004.
Enoki, M., Fujita, M., Nishizaki, T., Iikubo, S., Singh, D. K., Chang, S., Tranquada, J. M., & Yamada, K. (2013). Spin-stripe density varies linearly with the hole content in single-layer Bi2+xSr2-xCuO6+y cuprate superconductors. Physical review letters, 110(1), 017004. https://doi.org/10.1103/PhysRevLett.110.017004
Enoki, M, et al. "Spin-stripe density varies linearly with the hole content in single-layer Bi2+xSr2-xCuO6+y cuprate superconductors." Physical review letters vol. 110,1 (2013): 017004. doi: https://doi.org/10.1103/PhysRevLett.110.017004
Enoki M, Fujita M, Nishizaki T, Iikubo S, Singh DK, Chang S, Tranquada JM, Yamada K. Spin-stripe density varies linearly with the hole content in single-layer Bi2+xSr2-xCuO6+y cuprate superconductors. Phys Rev Lett. 2013 Jan 04;110(1):017004. doi: 10.1103/PhysRevLett.110.017004. Epub 2013 Jan 02. PMID: 23383829.
Copy Download .nbib Format: NLM
Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate.

The Journal of organic chemistry

Noji M, Ohno T, Fuji K, Futaba N, Tajima H, Ishii K.
PMID: 14629155
J Org Chem. 2003 Nov 28;68(24):9340-7. doi: 10.1021/jo034255h.

The combination of a secondary benzyl alcohol and a metal triflate (e.g., La, Yb, Sc, and Hf triflate) in nitromethane was a highly effective secondary-benzylation system. Secondary benzylation of carbon (aromatic compounds, olefins, an enol acetate), nitrogen (amide derivatives),...

Cite
Noji M, Ohno T, Fuji K, et al. Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate. J Org Chem. 2003;68(24):9340-7doi: 10.1021/jo034255h.
Noji, M., Ohno, T., Fuji, K., Futaba, N., Tajima, H., & Ishii, K. (2003). Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate. The Journal of organic chemistry, 68(24), 9340-7. https://doi.org/10.1021/jo034255h
Noji, Masahiro, et al. "Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate." The Journal of organic chemistry vol. 68,24 (2003): 9340-7. doi: https://doi.org/10.1021/jo034255h
Noji M, Ohno T, Fuji K, Futaba N, Tajima H, Ishii K. Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate. J Org Chem. 2003 Nov 28;68(24):9340-7. doi: 10.1021/jo034255h. PMID: 14629155.
Copy Download .nbib Format: NLM
9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling.

The Journal of organic chemistry

Tannaci JF, Noji M, McBee JL, Tilley TD.
PMID: 18788782
J Org Chem. 2008 Oct 17;73(20):7895-900. doi: 10.1021/jo8017268. Epub 2008 Sep 13.

9,10-Dichlorooctafluoroanthracene (1) reacts with aryl boronic acids and terminal alkynes under palladium-catalyzed cross-coupling conditions to afford 9,10-diaryloctafluoroanthracenes (2a-e) and 9,10-dialkynyloctafluoroanthracenes (6a,b), respectively. Optical spectroscopy and cyclic voltammetry indicate that octafluoro-9,10-di(thiophen-2-yl)anthracene (2d) exhibits donor-acceptor character and a LUMO energy level...

Cite
Tannaci JF, Noji M, McBee JL, et al. 9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling. J Org Chem. 2008;73(20):7895-900doi: 10.1021/jo8017268.
Tannaci, J. F., Noji, M., McBee, J. L., & Tilley, T. D. (2008). 9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling. The Journal of organic chemistry, 73(20), 7895-900. https://doi.org/10.1021/jo8017268
Tannaci, John F, et al. "9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling." The Journal of organic chemistry vol. 73,20 (2008): 7895-900. doi: https://doi.org/10.1021/jo8017268
Tannaci JF, Noji M, McBee JL, Tilley TD. 9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling. J Org Chem. 2008 Oct 17;73(20):7895-900. doi: 10.1021/jo8017268. Epub 2008 Sep 13. PMID: 18788782.
Copy Download .nbib Format: NLM
Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia.

Purinergic signalling

Sun X, Imai M, Nowak-Machen M, Guckelberger O, Enjyoji K, Wu Y, Khalpey Z, Berberat P, Munasinghe J, Robson SC.
PMID: 21656186
Purinergic Signal. 2011 Dec;7(4):427-34. doi: 10.1007/s11302-011-9239-6. Epub 2011 Jun 09.

Liver ischemia reperfusion injury is associated with both local damage to the hepatic vasculature and systemic inflammatory responses. CD39 is the dominant vascular endothelial cell ectonucleotidase and rapidly hydrolyses both adenosine triphosphate (ATP) and adenosine diphosphate to adenosine monophosphate....

Cite
Sun X, Imai M, Nowak-Machen M, et al. Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia. Purinergic Signal. 2011;7(4):427-34doi: 10.1007/s11302-011-9239-6.
Sun, X., Imai, M., Nowak-Machen, M., Guckelberger, O., Enjyoji, K., Wu, Y., Khalpey, Z., Berberat, P., Munasinghe, J., & Robson, S. C. (2011). Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia. Purinergic signalling, 7(4), 427-34. https://doi.org/10.1007/s11302-011-9239-6
Sun, Xiaofeng, et al. "Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia." Purinergic signalling vol. 7,4 (2011): 427-34. doi: https://doi.org/10.1007/s11302-011-9239-6
Sun X, Imai M, Nowak-Machen M, Guckelberger O, Enjyoji K, Wu Y, Khalpey Z, Berberat P, Munasinghe J, Robson SC. Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia. Purinergic Signal. 2011 Dec;7(4):427-34. doi: 10.1007/s11302-011-9239-6. Epub 2011 Jun 09. PMID: 21656186; PMCID: PMC3224647.
Copy Download .nbib Format: NLM
9,10-Dichlorooctafluoroanthracene as a building block for n-type organic semiconductors.

The Journal of organic chemistry

Tannaci JF, Noji M, McBee J, Tilley TD.
PMID: 17590045
J Org Chem. 2007 Jul 20;72(15):5567-73. doi: 10.1021/jo070404a. Epub 2007 Jun 23.

9,10-Dichlorooctafluoroanthracene (1) was synthesized from commercially available tetrafluorophthalic acid by an optimized solution-phase route. To establish 1 as a synthon for n-type organic semiconductors, the compound was reacted with phenylboronic acid under modified Suzuki-Miyaura coupling conditions to generate octafluoro-9,10-diphenylanthracene...

Cite
Tannaci JF, Noji M, McBee J, et al. 9,10-Dichlorooctafluoroanthracene as a building block for n-type organic semiconductors. J Org Chem. 2007;72(15):5567-73doi: 10.1021/jo070404a.
Tannaci, J. F., Noji, M., McBee, J., & Tilley, T. D. (2007). 9,10-Dichlorooctafluoroanthracene as a building block for n-type organic semiconductors. The Journal of organic chemistry, 72(15), 5567-73. https://doi.org/10.1021/jo070404a
Tannaci, John F, et al. "9,10-Dichlorooctafluoroanthracene as a building block for n-type organic semiconductors." The Journal of organic chemistry vol. 72,15 (2007): 5567-73. doi: https://doi.org/10.1021/jo070404a
Tannaci JF, Noji M, McBee J, Tilley TD. 9,10-Dichlorooctafluoroanthracene as a building block for n-type organic semiconductors. J Org Chem. 2007 Jul 20;72(15):5567-73. doi: 10.1021/jo070404a. Epub 2007 Jun 23. PMID: 17590045.
Copy Download .nbib Format: NLM
Analysis of renal function during telaprevir-based triple therapy for chronic hepatitis C.

Experimental and therapeutic medicine

Kohjima M, Kurokawa M, Enjoji M, Yoshimoto T, Nakamura T, Ohashi T, Fukuizumi K, Harada N, Murata Y, Matsunaga K, Kato M, Kotoh K, Nakamuta M.
PMID: 27168803
Exp Ther Med. 2016 May;11(5):1781-1787. doi: 10.3892/etm.2016.3133. Epub 2016 Mar 09.

Telaprevir (TVR) is used for the treatment of chronic hepatitis C in a combination therapy with pegylated-interferon and ribavirin. Although renal dysfunction is one of the critical adverse outcomes of this treatment, little is known regarding the mechanism of...

Cite
Kohjima M, Kurokawa M, Enjoji M, et al. Analysis of renal function during telaprevir-based triple therapy for chronic hepatitis C. Exp Ther Med. 2016;11(5):1781-1787doi: 10.3892/etm.2016.3133.
Kohjima, M., Kurokawa, M., Enjoji, M., Yoshimoto, T., Nakamura, T., Ohashi, T., Fukuizumi, K., Harada, N., Murata, Y., Matsunaga, K., Kato, M., Kotoh, K., & Nakamuta, M. (2016). Analysis of renal function during telaprevir-based triple therapy for chronic hepatitis C. Experimental and therapeutic medicine, 11(5), 1781-1787. https://doi.org/10.3892/etm.2016.3133
Kohjima, Motoyuki, et al. "Analysis of renal function during telaprevir-based triple therapy for chronic hepatitis C." Experimental and therapeutic medicine vol. 11,5 (2016): 1781-1787. doi: https://doi.org/10.3892/etm.2016.3133
Kohjima M, Kurokawa M, Enjoji M, Yoshimoto T, Nakamura T, Ohashi T, Fukuizumi K, Harada N, Murata Y, Matsunaga K, Kato M, Kotoh K, Nakamuta M. Analysis of renal function during telaprevir-based triple therapy for chronic hepatitis C. Exp Ther Med. 2016 May;11(5):1781-1787. doi: 10.3892/etm.2016.3133. Epub 2016 Mar 09. PMID: 27168803; PMCID: PMC4840744.
Copy Download .nbib Format: NLM
Lactate dehydrogenase production in hepatocytes is increased at an early stage of acute liver failure.

Experimental and therapeutic medicine

Kotoh K, Kato M, Kohjima M, Tanaka M, Miyazaki M, Nakamura K, Enjoji M, Nakamuta M, Takayanagi R.
PMID: 22977488
Exp Ther Med. 2011 Mar;2(2):195-199. doi: 10.3892/etm.2011.197. Epub 2011 Jan 19.

Although the mechanism involved in acute liver failure (ALF) has not yet been clarified, microcirculatory disturbance in the liver appears to play a pivotal role in the progression of this disease. To confirm the existence of hepatic hypoxic conditions,...

Cite
Kotoh K, Kato M, Kohjima M, et al. Lactate dehydrogenase production in hepatocytes is increased at an early stage of acute liver failure. Exp Ther Med. 2011;2(2):195-199doi: 10.3892/etm.2011.197.
Kotoh, K., Kato, M., Kohjima, M., Tanaka, M., Miyazaki, M., Nakamura, K., Enjoji, M., Nakamuta, M., & Takayanagi, R. (2011). Lactate dehydrogenase production in hepatocytes is increased at an early stage of acute liver failure. Experimental and therapeutic medicine, 2(2), 195-199. https://doi.org/10.3892/etm.2011.197
Kotoh, Kazuhiro, et al. "Lactate dehydrogenase production in hepatocytes is increased at an early stage of acute liver failure." Experimental and therapeutic medicine vol. 2,2 (2011): 195-199. doi: https://doi.org/10.3892/etm.2011.197
Kotoh K, Kato M, Kohjima M, Tanaka M, Miyazaki M, Nakamura K, Enjoji M, Nakamuta M, Takayanagi R. Lactate dehydrogenase production in hepatocytes is increased at an early stage of acute liver failure. Exp Ther Med. 2011 Mar;2(2):195-199. doi: 10.3892/etm.2011.197. Epub 2011 Jan 19. PMID: 22977488; PMCID: PMC3440653.
Copy Download .nbib Format: NLM
Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins.

Organic & biomolecular chemistry

Hayashi S, Takamatsu R, Takeda S, Noji M, Takanami T.
PMID: 33290491
Org Biomol Chem. 2020 Dec 28;18(48):9791-9795. doi: 10.1039/d0ob02262d. Epub 2020 Dec 08.

A convenient method for the preparation of meso,β-dual-functionalized porphyrin was developed. The bromination of zincatedβ-silylporphyrin with NBS selectively yielded meso-bromo-β-silylporphyrin, whereas, the bromination of free-baseβ-silylporphyrin selectively yielded β-bromoporphyrin via an ipso-substitution of the silyl group. These meso,β-dual-functionalized porphyrins could...

Cite
Hayashi S, Takamatsu R, Takeda S, et al. Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins. Org Biomol Chem. 2020;18(48):9791-9795doi: 10.1039/d0ob02262d.
Hayashi, S., Takamatsu, R., Takeda, S., Noji, M., & Takanami, T. (2020). Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins. Organic & biomolecular chemistry, 18(48), 9791-9795. https://doi.org/10.1039/d0ob02262d
Hayashi, Satoshi, et al. "Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins." Organic & biomolecular chemistry vol. 18,48 (2020): 9791-9795. doi: https://doi.org/10.1039/d0ob02262d
Hayashi S, Takamatsu R, Takeda S, Noji M, Takanami T. Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins. Org Biomol Chem. 2020 Dec 28;18(48):9791-9795. doi: 10.1039/d0ob02262d. Epub 2020 Dec 08. PMID: 33290491.
Copy Download .nbib Format: NLM
Proton-accelerated Lewis acid catalysis for stereo- and regioselective isomerization of epoxides to allylic alcohols.

Chemical communications (Cambridge, England)

Noji M, Baba M, Hirabe R, Hayashi S, Takanami T.
PMID: 34179905
Chem Commun (Camb). 2021 Jul 20;57(58):7104-7107. doi: 10.1039/d1cc02840e.

The isomerization of epoxides to allylic alcohols was developed via proton-accelerated Lewis acid catalysis. The addition of tBuOH as a proton source is the key to the efficient catalytic cycle. Trisubstituted epoxides, including enantioenriched derivatives, were selectively converted to...

Cite
Noji M, Baba M, Hirabe R, et al. Proton-accelerated Lewis acid catalysis for stereo- and regioselective isomerization of epoxides to allylic alcohols. Chem Commun (Camb). 2021;57(58):7104-7107doi: 10.1039/d1cc02840e.
Noji, M., Baba, M., Hirabe, R., Hayashi, S., & Takanami, T. (2021). Proton-accelerated Lewis acid catalysis for stereo- and regioselective isomerization of epoxides to allylic alcohols. Chemical communications (Cambridge, England), 57(58), 7104-7107. https://doi.org/10.1039/d1cc02840e
Noji, Masahiro, et al. "Proton-accelerated Lewis acid catalysis for stereo- and regioselective isomerization of epoxides to allylic alcohols." Chemical communications (Cambridge, England) vol. 57,58 (2021): 7104-7107. doi: https://doi.org/10.1039/d1cc02840e
Noji M, Baba M, Hirabe R, Hayashi S, Takanami T. Proton-accelerated Lewis acid catalysis for stereo- and regioselective isomerization of epoxides to allylic alcohols. Chem Commun (Camb). 2021 Jul 20;57(58):7104-7107. doi: 10.1039/d1cc02840e. PMID: 34179905.
Copy Download .nbib Format: NLM
Insulin-stimulated adipocytes secrete lactate to promote endothelial fatty acid uptake and transport.

Journal of cell science

Ibrahim A, Neinast MD, Li K, Noji M, Kim B, Bornstein MR, Mohammed R, Wellen KE, Arany Z.
PMID: 34779480
J Cell Sci. 2021 Nov 15; doi: 10.1242/jcs.258964. Epub 2021 Nov 15.

Insulin stimulates adipose tissue to extract fatty acids from circulation and sequester them inside adipose cells. How fatty acids are transported across the capillary endothelial barrier, or how this process is regulated, remains unclear. We modeled the relationship of...

Cite
Ibrahim A, Neinast MD, Li K, et al. Insulin-stimulated adipocytes secrete lactate to promote endothelial fatty acid uptake and transport. J Cell Sci. 2021;doi: 10.1242/jcs.258964.
Ibrahim, A., Neinast, M. D., Li, K., Noji, M., Kim, B., Bornstein, M. R., Mohammed, R., Wellen, K. E., & Arany, Z. (2021). Insulin-stimulated adipocytes secrete lactate to promote endothelial fatty acid uptake and transport. Journal of cell science, . https://doi.org/10.1242/jcs.258964
Ibrahim, Ayon, et al. "Insulin-stimulated adipocytes secrete lactate to promote endothelial fatty acid uptake and transport." Journal of cell science vol. (2021). doi: https://doi.org/10.1242/jcs.258964
Ibrahim A, Neinast MD, Li K, Noji M, Kim B, Bornstein MR, Mohammed R, Wellen KE, Arany Z. Insulin-stimulated adipocytes secrete lactate to promote endothelial fatty acid uptake and transport. J Cell Sci. 2021 Nov 15; doi: 10.1242/jcs.258964. Epub 2021 Nov 15. PMID: 34779480.
Copy Download .nbib Format: NLM
Showing 25 to 36 of 90 entries